4-((1,3,6,7-Tetramethoxyxanthone-4-yl)-sulfonyl)-(2R,6S)-2,6-dimethyl-morpholine

ID: ALA1096715

PubChem CID: 46887524

Max Phase: Preclinical

Molecular Formula: C23H27NO9S

Molecular Weight: 493.53

Molecule Type: Small molecule

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  COc1cc2oc3c(S(=O)(=O)N4C[C@@H](C)O[C@@H](C)C4)c(OC)cc(OC)c3c(=O)c2cc1OC

Standard InChI:  InChI=1S/C23H27NO9S/c1-12-10-24(11-13(2)32-12)34(26,27)23-19(31-6)9-18(30-5)20-21(25)14-7-16(28-3)17(29-4)8-15(14)33-22(20)23/h7-9,12-13H,10-11H2,1-6H3/t12-,13+

Standard InChI Key:  GLWCNHCKGJYPPI-BETUJISGSA-N

Molfile:  

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M  END

Associated Targets(Human)

SOAT1 Tchem Acyl coenzyme A:cholesterol acyltransferase 1 (857 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Calculated Properties

Molecular Weight: 493.53Molecular Weight (Monoisotopic): 493.1407AlogP: 2.78#Rotatable Bonds: 6
Polar Surface Area: 113.74Molecular Species: NEUTRALHBA: 9HBD:
#RO5 Violations: HBA (Lipinski): 10HBD (Lipinski): #RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: CX LogP: 2.00CX LogD: 2.00
Aromatic Rings: 3Heavy Atoms: 34QED Weighted: 0.48Np Likeness Score: -0.06

References

1. Hu H, Liao H, Zhang J, Wu W, Yan J, Yan Y, Zhao Q, Zou Y, Chai X, Yu S, Wu Q..  (2010)  First identification of xanthone sulfonamides as potent acyl-CoA:cholesterol acyltransferase (ACAT) inhibitors.,  20  (10): [PMID:20403694] [10.1016/j.bmcl.2010.03.101]
2. Pokhrel, Laxman and 5 more authors.  2012-10-25  Inhibition of Acyl-CoA: cholesterol acyltransferase (ACAT), overexpression of cholesterol transporter gene, and protection of amyloid β (Aβ) oligomers-induced neuronal cell death by tricyclic pyrone molecules.  [PMID:23025824]
3. Ting, Pauline C PC and 10 more authors.  2013-02-15  Lead optimization of a pyridine-carboxamide series as DGAT-1 inhibitors.  [PMID:23317570]
4. Eguchi, Keisuke K and 10 more authors.  2013-07-01  Manzamine A, a marine-derived alkaloid, inhibits accumulation of cholesterol ester in macrophages and suppresses hyperlipidemia and atherosclerosis in vivo.  [PMID:23665143]

Source